Identification of the NH2-terminal blocking group of calcineurin B as myristic acid

FEBS Lett. 1982 Dec 27;150(2):314-8. doi: 10.1016/0014-5793(82)80759-x.

Abstract

The NH2-terminal blocking group of the Ca2+-binding B-subunit of calcineurin (protein phosphatase-2B) has been identified as myristic acid by fast atom bombardment mass spectrometry and gas chromatography. The sequence, myristyl-Gly-Asn-Glu-Ala-, is very similar to that of the catalytic subunit of cyclic AMP-dependent protein kinase, the only other protein known to contain this fatty acid. This finding, and the elution of all myristyl peptides at 57% acetonitrile on reverse phase HPLC, may facilitate the identification of other proteins with this blocking group.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / analysis
  • Animals
  • Brain Chemistry*
  • Calcium-Binding Proteins / isolation & purification*
  • Calmodulin-Binding Proteins
  • Cattle
  • Chromatography, Gas
  • Mass Spectrometry
  • Myristic Acid
  • Myristic Acids / analysis*
  • Nerve Tissue Proteins / isolation & purification*

Substances

  • Amino Acids
  • Calcium-Binding Proteins
  • Calmodulin-Binding Proteins
  • Myristic Acids
  • Nerve Tissue Proteins
  • Myristic Acid